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Synthesis of β‐Alkoxy Amines from Alkenes, Sulfonyl Azides, and Alcohols though Copper‐Catalyzed Three‐Component Tandem Reactions via Regioselective Ring‐Opening of Aziridine Intermediates

Synthesis of β‐Alkoxy Amines from Alkenes, Sulfonyl Azides, and Alcohols though Copper‐Catalyzed... A copper‐catalyzed three‐component tandem reaction of alkenes, sulfonyl azides, and alcohols is described. This straightforward transformation provides a practical method for the synthesis of valuable β‐alkoxy amines from easily accessible starting materials under comparative cheap copper catalysis without external ligands though regioselective ring‐opening reaction of aziridine intermediates. This reaction has a broad functional groups tolerance and the yields are generally good. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Asian Journal of Organic Chemistry Wiley

Synthesis of β‐Alkoxy Amines from Alkenes, Sulfonyl Azides, and Alcohols though Copper‐Catalyzed Three‐Component Tandem Reactions via Regioselective Ring‐Opening of Aziridine Intermediates

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References (40)

Publisher
Wiley
Copyright
© 2021 Wiley‐VCH GmbH
ISSN
2193-5807
eISSN
2193-5815
DOI
10.1002/ajoc.202100087
Publisher site
See Article on Publisher Site

Abstract

A copper‐catalyzed three‐component tandem reaction of alkenes, sulfonyl azides, and alcohols is described. This straightforward transformation provides a practical method for the synthesis of valuable β‐alkoxy amines from easily accessible starting materials under comparative cheap copper catalysis without external ligands though regioselective ring‐opening reaction of aziridine intermediates. This reaction has a broad functional groups tolerance and the yields are generally good.

Journal

Asian Journal of Organic ChemistryWiley

Published: May 1, 2021

Keywords: ; ; ; ;

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